Medical Writer in Costello Medical's Medical Communications team specializing in scientific publications and communication of clinical trial data. Collaborating with clients to deliver high - quality scientific materials.
About the role
- Medical Writer I role focusing on document management within Veeva systems for clinical projects. Supporting compliance and adherence to GxP guidelines while collaborating with stakeholders.
Responsibilities
- Support accurate and compliant document filing within Veeva RIM
- Perform eTMF filing activities while adhering to GxP guidelines
- Manage document handling activities within Veeva
- Ensure documents meet quality and integrity standards
- Categorize documents systematically for retrieval
Requirements
- 1–2 years of experience in ETMF filing and Document management systems
- Experience in Filing documents based on Versions, Metadata and Filing structure
- Experience of Veeva (Viva) RIM / Veeva Clinical
- Good understanding of GxP guidelines
- Excellent communication skills in English
Benefits
- Career development and progression
- Supportive and engaged line management
- Technical and therapeutic area training
- Peer recognition and total rewards program
- Total Self culture promoting authenticity
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
RN specializing in clinical documentation integrity for pediatric patients at Connecticut Children's. Collaborating with healthcare providers to enhance documentation standards and accuracy.
Principal Medical Writer at IQVIA producing inspection - ready Clinical Study Reports for Phase 1 studies. Collaborating with teams to ensure compliance with regulatory and internal guidelines while maintaining document quality.
Principal Digital Medical Writer translating complex scientific evidence into engaging medical communications. Leading evidence synthesis projects and collaborating with digital, data, and design teams in a hybrid role.
Medical Writer creating and reviewing regulatory and public - facing documents. Supporting clinical and regulatory strategies with an emphasis on compliance and health literacy principles.
Senior Medical Writer overseeing high - quality clinical and regulatory documents at Ipsen, a biopharmaceutical company. Leading cross - functional teams and contributing to regulatory strategy while ensuring compliance and innovation in medical writing practices.
Medical Copywriter creating pharmaceutical promotional content for a global digital agency. Developing strategies and overseeing editorial quality for marketing communications in the life sciences sector.
CDI Nurse assisting GBMC Health Partners with documentation improvement efforts. Collaborating with physicians and clinicians on patient records and risk management.
Clinical Documentation Specialist working with healthcare teams to ensure accurate medical record documentation. Aiding in compliance and coding education for clinical documentation improvement.
Medical Writer at Real Chemistry developing scientific copy for healthcare communications. Collaborating with medical writers and adhering to style guidelines for various projects.